ID

34571

Description

Reducing Atrial Pacing Rate to Reduce Atrial Fibrillation in Patients With Sick Sinus Syndrome.; ODM derived from: https://clinicaltrials.gov/show/NCT02034526

Link

https://clinicaltrials.gov/show/NCT02034526

Keywords

  1. 1/19/19 1/19/19 -
Copyright Holder

GSK group of companies

Uploaded on

January 19, 2019

DOI

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License

Creative Commons BY-NC 3.0

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Eligibility Sinus Node Disease NCT02034526

Eligibility Sinus Node Disease NCT02034526

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
sick sinus syndrome and indication for first-time implantation of a ddd pacemaker: symptomatic sinus pauses (>2 sec) or bradycardia with or without paroxysmal af.
Description

ID.1

Data type

boolean

age ≥18 years.
Description

ID.2

Data type

boolean

patient informed consent.
Description

ID.3

Data type

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
permanent or persisting (>7 days) af prior to implantation.
Description

ID.4

Data type

boolean

persisting symptomatic sinus bradycardia and/or chronotropic incompetence where ddd-pacing at a frequency of >40 bpm is indicated (verified with long term ecg monitoring).
Description

ID.5

Data type

boolean

persisting second or third degree av block.
Description

ID.6

Data type

boolean

life expectancy <2 years.
Description

ID.7

Data type

boolean

participation in another interventional research study.
Description

ID.8

Data type

boolean

indication for implantable cardioverter defibrillator (icd) or cardiac resynchronization therapy (crt).
Description

ID.9

Data type

boolean

pregnancy.
Description

ID.10

Data type

boolean

Similar models

Eligibility Sinus Node Disease NCT02034526

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
sick sinus syndrome and indication for first-time implantation of a ddd pacemaker: symptomatic sinus pauses (>2 sec) or bradycardia with or without paroxysmal af.
boolean
ID.2
Item
age ≥18 years.
boolean
ID.3
Item
patient informed consent.
boolean
Item Group
C0680251 (UMLS CUI)
ID.4
Item
permanent or persisting (>7 days) af prior to implantation.
boolean
ID.5
Item
persisting symptomatic sinus bradycardia and/or chronotropic incompetence where ddd-pacing at a frequency of >40 bpm is indicated (verified with long term ecg monitoring).
boolean
ID.6
Item
persisting second or third degree av block.
boolean
ID.7
Item
life expectancy <2 years.
boolean
ID.8
Item
participation in another interventional research study.
boolean
ID.9
Item
indication for implantable cardioverter defibrillator (icd) or cardiac resynchronization therapy (crt).
boolean
ID.10
Item
pregnancy.
boolean

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